Rod Atkins
Global CAPA & Regulatory Compliance SME-Market Quality, Process and Complaint Teams at Global Medical Device Client | Jupiter, Florida, United States
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Global CAPA & Regulatory Compliance SME-Market Quality, Process and Complaint Teams at Global Medical Device Client in January 2023 to December 2024
Quality Systems Consultant for OOS/Deviation investigation for Process, Product & Post Market NCs at ProPharma Group in June 2022 to December 2022
Director Of Quality at Accelus in April 2021 to June 2022
Quality Assurance Manager at Zimmer Biomet Dental in November 2019 to May 2021
CAPA Manager at Zimmer Biomet Dental in April 2017 to October 2019
Supplier Quality Validations Consultant at Zimmer Biomet in August 2016 to April 2017
Site CAPA Program Lead & QMS Remediation Project Manager (PMO) at Johnson & Johnson MedTech in September 2012 to July 2016
Senior Quality Systems Consultant-OOS/Deviation Investigation-FDA Remediation Project at Pfizer in May 2012 to October 2012
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Production Planning
Inventory Management
KPI Reporting
Investigation
team colaboration
Employee Training
Supplier Performance
Quality Process Development
Manufacturing Operations
liquid pharmaceuticals
Supplier Quality Management
Deviation Management
Process Validation
Team Leadership
Manufacturing Process Improvement
VOE
Administration
A3 Problem Solving
Project Planning
QMS
External Audits
Product Development
Recall
HHA/HHE
FDA GMP
Internal Audits
Supplier Evaluation
Cleaning Validation
System Administration
Pharmaceutics
Pellets
Medication Dispensing
Tablet Compression
Validation Protocol
A3
Risk Assessment
Risk Management
Mergers & Acquisitions (M&A)
Remediation
Problem Solving
Trend Analysis
Financial Analysis
Quality Systems Design
Communication
Supply Agreements
Product Life Cycle
Contract Manufacturing
SCAR
Management Review
Negotiation
Cellular Manufacturing
FDA
Lean Manufacturing
ISO
Food
Medical Devices
CAPA
GMP
Project Management
Quality System
Quality Auditing
Quality Assurance
Sop
HACCP
DMAIC
Design Control
MRP
21 CFR Part 11
Validation
ISO 13485
Pharmaceutical Industry
Change Control
Change Management
Quality Control
Kaizen
Process Improvement
Continuous Improvement
Six Sigma
Supply Chain
Cross-functional Team Leadership
FMEA
Process Engineering
Quality Management
Supply Chain Management
Manufacturing
Software Documentation
Root Cause Analysis
Supplier Quality
Technology Transfer
Leadership
V&V
Value Stream Mapping
SPC
Regulatory Requirements
Operational Excellence
R&D
Process Simulation
ISO 14971
Program Management
Design of Experiments
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What is Rod Atkins email address?
Email Rod Atkins at [email protected] and [email protected]. This email is the most updated Rod Atkins's email found in 2026.
How to contact Rod Atkins?
To contact Rod Atkins send an email to [email protected] or [email protected].
What company does Rod Atkins work for?
Rod Atkins works for Global Medical Device Client
What is Rod Atkins's role at Global Medical Device Client?
Rod Atkins is Global CAPA & Regulatory Compliance SME-Market Quality, Process and Complaint Teams
What is Rod Atkins's Phone Number?
Rod Atkins's phone (305) ***-*313
What industry does Rod Atkins work in?
Rod Atkins works in the Medical Device industry.
Rod Atkins Email Addresses
Rod Atkins Phone Numbers
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